Cyproheptadine Hydrochloride Tablet
Product Images NDC 81279-129

3 FDA label images from Pangea Pharmaceuticals, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Cyproheptadine Hydrochloride (NDC 81279-129). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pangea Pharmaceuticals, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Image Description (Chemsture)

Image Description (Chemsture)
Chemical structure diagram of cyproheptadine hydrochloride, displaying its molecular formula C21H21N·HCl and molecular weight of 350.89.*
FDA Label Image

30 Tablets Bottle Label (Tablet 30c)

30 Tablets Bottle Label (Tablet 30c)
The label for Cyproheptadine Hydrochloride Tablets, USP (Cyprolara) 2 mg by Pangea Pharmaceuticals, LLC. The label states each tablet contains 2 mg cyproheptadine HCl and comes in a package of 30 tablets for oral use. It includes storage instructions, a bar code, and a caution to keep medications out of children's reach.*
FDA Label Image

60 Tablets Bottle Label (Tablet 60c)

60 Tablets Bottle Label (Tablet 60c)
Label for Cyproheptadine Hydrochloride 2 mg oral tablets from Pangea Pharmaceuticals. The label indicates the product name Cyprolara, strength of 2 mg per tablet, and bottle count of 60 tablets. It includes storage instructions at controlled room temperature (20° to 25°C) and a warning to keep medications out of children's reach. The label features a barcode, manufacturer details, and a Made in USA flag.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.